A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059562



Internal ID19148781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53542631..53566028hg38UCSC Ensembl
Innerchr16:53576543..53599940hg19UCSC Ensembl
Innerchr16:52134044..52157441hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3823398
hg1923398
hg1823398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559265
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059562
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer